Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F114/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
  • C08F114/02—Monomers containing chlorine
  • C08F114/04—Monomers containing two carbon atoms
  • C08F114/06—Vinyl chloride
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
  • Y10S526/909—Polymerization characterized by particle size of product

Definitions

• the present invention relates to a process for the suspension polymerisation of vinyl halides.
• aqueous dispersion polymerisation commonly used for vinyl halides. These are often known as suspension, emulsion and microsuspension.
• Suspension polymerisation uses a monomer soluble free radical initiator and the dispersion droplet size is large, giving polymer particles of a size greater than about 50 ⁇ m, which can be separated from the dispersion by centrifuging or filtering.
• the dispersion is stabilised by such substances as cellulose ethers, polyvinyl alcohol, gelatin and finely divided inorganic solids such as hydroxy apatite, which are known as dispersants or suspending agents and are not considered to be true surfactants. Stirring is required during polymerisation in addition to the stabilisers to prevent the dispersion agglomerating and from undergoing sedimentation.
• Emulsion polymerisation uses water soluble initiators and the polymer is formed as a latex of particles usually of less than 1 ⁇ m diameter which cannot be separated from the aqueous phase by centrifuging or filtering.
• True surfactants are used to stabilise the dispersions, which are normally stable on standing, although the polymerisation is stirred.
• Microsuspension polymerisations like suspensions, use monomer soluble initiators but the polymer is formed as a latex of particles, usually less than 2 ⁇ m diameter but sometimes up to as much as 20 ⁇ m which cannot be separated from the aqueous phase by centrifuging or filtering. These latices are normally isolated by spray drying to give polymers which can form pastes when mixed with plasticisers.
• True surfactants are used as stabilisers and often a system containing more than one surfactant or surfactants and surfactant modifiers are used. These dispersions unlike suspensions or emulsions cannot simply be produced by stirring the monomer and water in the presence of the surfactant using the normal degree of agitation required during polymerisation.
• British patent specification No. 1,348,426 relates to a batch process for the suspension polymerisation of vinyl chloride in which vinyl chloride is fed in continuously over an initial period of polymerisation, the addition of monomer being stopped, at the latest after 70% of the total vinyl chloride introduced has reacted i.e. the addition of vinyl chloride is not continued after the pressure drop. It is stated that where the continuous addition of vinyl chloride is continued after the pressure drop the number of specks in the product is increased but the other properties are not affected. A similar result is obtained if the process is operated on a semi-continuous basis by withdrawing a portion of the reaction mixture at the pressure drop and replacing it with a fresh charge of monomer and water.
• the present invention is a batch process for the homo-polymerisation of a vinyl halide monomer which comprises homo-polymerising the monomer in aqueous suspension in the presence of a monomer soluble free radical initiator until the start of the pressure drop and thereafter adding not more than 50% by weight of initial vinyl chloride of fresh vinyl halide over not more than 15 minutes in a period in which the conversion is in the range 70% to 80% by weight of the monomer initially added, completing the polymerisation, and only then recovering the monomer.
• Any polymerisable vinyl halide-containing monomeric material may be used, but the preferred monomer is vinyl chloride.
• the vinyl halide added to the polymerization after the pressure drop is bulk monomer, that is vinyl halide which is not dispersed or suspended in water.
• the polymerisation is carried out in a monomeric material-in-water suspension, i.e. in a turbulence-stabilised dispersion containing suspending agent and using a monomer soluble free radical initiator.
• the monomeric material to water phase ratio is not critical provided that sufficient water is present to allow the monomeric material to be maintained in dispersion therein.
• this ratio is in the range 1:1 to 1:3 by weight, and more preferably 1:1.1 to 1:2.5 by weight.
• the polymerisation process may be carried out at conventional temperatures used for the suspension polymerisation of vinyl chloride.
• a temperature in the range +5° to +75°C is used.
• the polymerisation temperature may be varied during the reaction.
• Suitable initiators include lauroyl peroxide, caprylyl peroxide, benzoyl peroxide, tertiary butyl peroxypivalate, 2-azobisisobutyronitrile, peroxydicarbonates such as ditertiary-butylcyclohexylperoxydicarbonate, diethyl peroxydicarbonate, dicyclohexylperoxydicarbonate and diisopropylperoxydicarbonate.
• Suitable initiators are those which are formed ⁇ in situ ⁇ in the reaction medium; for example, the initiator formed by the reaction of a chloroformate, such as ethyl chloroformate or isopropylchloroformate, and hydrogen peroxide under alkaline conditions.
• a chloroformate such as ethyl chloroformate or isopropylchloroformate
• Combinations of the above initiators may also be used.
• the amount of initiator used may be similar to that used in conventional vinyl halide suspension polymerisation processes. Fresh initiator may also be added together with the extra monomeric material which is added to the polymerisation system during the pressure-drop period.
• Suitable suspending agents include insoluble inorganic phosphates such as hydroxyapatite and organic colloids such as cellulose ethers, gelatin or incompletely hydrolysed polyvinylacetates.
• the polymerisation is carried out in a closed vessel, generally under autogenous pressure.
• the additional vinyl halide containing monomeric material is preferably added in one increment at or shortly after the commencement of the pressure drop, i.e. before the pressure has dropped by more than about 30 psi or preferably 15 psi, in order to gain the maximum advantage with respect to increase of vessel productivity for a given reaction time.
• the part addition of vinyl halide during the polymerisation is most conveniently carried out by adding all the vinyl halide at once so reducing the time spent supervising the addition to the minimum. It may not be physically possible to add all the vinyl halide at once due to limitations on the size of pipes etc, but in any case the addition must take place over not more than 15 minutes, and preferably over not more than 10 minutes. It is particularly preferred to carry out the addition of the vinyl halide monomer over not more than 5 minutes. The addition may be delayed after the pressure drop, but its effectiveness is reduced and the polymerisation time is more extended. The addition of monomer must take place during the period in which conversion of the monomer is in the range 70% to 80% of the monomer originally present.
• the additional monomer will generally raise the pressure to the saturated vapour pressure again and this is preferred.
• the amount added is from 2 to 30% of the initial change.
• the polymerisation is allowed to proceed after the addition of the vinyl halide to the degree of conversion of total vinyl halide to polymer which is normal for suspension polymerisation so completing the polymerisation.
• a conventional vinyl chloride suspension polymerisation vessel was charged with water (131 parts by weight), an aqueous solution of a cellulose ether dispersant system (0.22 parts), and an initiator system comprising di-t-butylcyclohexylperoxydicarbonate (0.03 parts) and caprylyl peroxide (0.03 parts).
• the system was maintained at pH ca 7 by use of a pH adjuster.
• the polymerisation vessel was sealed, evacuated, and vinyl chloride (100 parts) was introduced into the vessel at room temperature.
• the temperature of the agitated vinyl chloride-in-water turbulence-stabilised dispersion was then increased to 58°C, and the polymerisation was allowed to proceed at this temperature until the pressure within the reaction vessel had fallen by 28 psi from the maximum pressure reached during the polymerisation (i.e. from ca 128 psig).
• a further suspension polymerisation was carried out according to the procedure outlined for Example 1, except that a vinyl chloride monomer post-addition stage, after a pressure-drop of 28 psig had occurred, was not carried out.
• the total time for the polymerisation was ca 61/2 hours.
• the bulk density of the dried PVC homopolymer product was 548 kg/m 3 .
• a conventional vinyl chloride suspension polymerisation vessel (not the one used in Example 1), was charged with town's water (170 parts by weight), an aqueous cellulose ether dispersant system (0.22 parts) and an initiator system comprising di-t-butylcyclohexylperoxydicarbonate (0.03 parts) and caprylyl peroxide (0.0247 parts).
• Vinyl chloride was introduced into the reactor and polymerised as in Example 1.
• Vinyl chloride (30 parts by weight) was fed in at the commencement of the pressure drop over a period of 3 minutes. This was sufficient to restore the pressure to its value before the start of the pressure drop. Polymerisation was continued as in Example 1. The results are given in the Table.
• Example 3 In a comparative Example not according to the invention an experiment was carried out as in Example 3 but with the monomer added at a conversion of 90% of the original charge of monomer, instead of at the commencement of the pressure drop. The results are shown in the Table.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Polymerisation Methods In General (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

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• 1973
  • 1973-12-26 GB GB30183/73A patent/GB1489866A/en not_active Expired
• 1974
  • 1974-12-18 NL NLAANVRAGE7416495,A patent/NL177023C/xx not_active IP Right Cessation
  • 1974-12-18 NL NL7416494A patent/NL7416494A/xx not_active Application Discontinuation
  • 1974-12-20 SE SE7416179A patent/SE407069B/xx unknown
  • 1974-12-20 SE SE7416180A patent/SE413192B/xx unknown
  • 1974-12-20 US US05/534,790 patent/US3954698A/en not_active Expired - Lifetime
  • 1974-12-20 US US05/534,798 patent/US3980603A/en not_active Expired - Lifetime
  • 1974-12-23 NO NO744679A patent/NO141719C/no unknown
  • 1974-12-23 DE DE19742461082 patent/DE2461082A1/de not_active Ceased
  • 1974-12-23 NO NO744680A patent/NO744680L/no unknown
  • 1974-12-23 DE DE19742461083 patent/DE2461083A1/de active Granted
  • 1974-12-24 FR FR7442687A patent/FR2256183B1/fr not_active Expired
  • 1974-12-24 FR FR7442688A patent/FR2256184B1/fr not_active Expired
  • 1974-12-24 BE BE151922A patent/BE823850A/xx not_active IP Right Cessation
  • 1974-12-24 BE BE151921A patent/BE823849A/xx not_active IP Right Cessation
  • 1974-12-26 JP JP751965A patent/JPS5937283B2/ja not_active Expired
  • 1974-12-26 JP JP751964A patent/JPS5928209B2/ja not_active Expired

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